tetano
Editor, Senior Moderator
Avian Dis
. 2024 Mar;68(1):43-51.
doi: 10.1637/aviandiseases-D-23-00029. Mapping Genetic Markers Associated with Antigenicity and Host Range in H9N2 Influenza A Viruses Infecting Poultry in Pakistan
Faisal Amin[SUP] 1 2 [/SUP], Nadia Mukhtar[SUP] 1 [/SUP], Muzaffar Ali[SUP] 1 [/SUP], Rehman Shehzad[SUP] 2 3 [/SUP], Saima Ayub[SUP] 4 [/SUP], Asim Aslam[SUP] 1 [/SUP], Ali Ahmed Sheikh[SUP] 1 [/SUP], Bakht Sultan[SUP] 2 [/SUP], Muhammad Danish Mahmood[SUP] 5 [/SUP], Muhammad Furqan Shahid[SUP] 1 6 [/SUP], Saima Yaqub[SUP] 1 [/SUP], Hassaan Bin Aslam[SUP] 1 [/SUP], Muhammad Waqar Aziz[SUP] 1 [/SUP], Tahir Yaqub[SUP] 7 [/SUP]
Affiliations
in English, Spanish
The aim of the current study was to map the genetic diversity in the haemagglutinin (HA) glycoprotein of influenza A viruses (IAVs) of the H9N2 subtype. Twenty-five H9N2 IAVs were isolated from broiler chickens from March to July 2019. The HA gene was amplified, and phylogenetic analysis was performed to determine the evolutionary relationship. Important antigenic amino acid residues of HA attributed to immune escape and zoonotic potential were compared among H9N2 IAVs. Phylogenetic analysis revealed that sublineage B2 under the G1 lineage in Pakistan was found to be diversified, and newly sequenced H9N2 isolates were nested into two clades (A and B). Mutations linked to the antigenic variation and potential immune escape were observed as G72E (1/25, 4%), A180T (3/25, 12%), and A180V (1/25, 4%). A twofold significant reduction (P < 0.01) in log[SUB]2[/SUB] hemagglutination inhibition titers was observed with H9N2 IAV naturally harboring amino acid V180 instead of A180 in HA protein. Moreover, in the last 20 years, complete substitution at residues (T127D, D135N, and L150N) and partial substitution at residues (72, 74, 131, 148, 180, 183, 188, 216, 217, and 249, mature H9 HA numbering) associated with changes in antigenicity were observed. The presence of L216 in all H9N2 IAV isolates and T/V180 in four isolates in the receptor-binding site reveals the potential of these viruses to cross the species barrier to infect human or mammals. The current study observed the circulation of antigenically diverse H9N2 IAV variants that possess potential mutations that can escape the host immune system.
Keywords: H9N2 influenza A virus; HA protein; antigenic sites; mammalian adaptation; phylogenetic analysis; potential mutations.
. 2024 Mar;68(1):43-51.
doi: 10.1637/aviandiseases-D-23-00029. Mapping Genetic Markers Associated with Antigenicity and Host Range in H9N2 Influenza A Viruses Infecting Poultry in Pakistan
Faisal Amin[SUP] 1 2 [/SUP], Nadia Mukhtar[SUP] 1 [/SUP], Muzaffar Ali[SUP] 1 [/SUP], Rehman Shehzad[SUP] 2 3 [/SUP], Saima Ayub[SUP] 4 [/SUP], Asim Aslam[SUP] 1 [/SUP], Ali Ahmed Sheikh[SUP] 1 [/SUP], Bakht Sultan[SUP] 2 [/SUP], Muhammad Danish Mahmood[SUP] 5 [/SUP], Muhammad Furqan Shahid[SUP] 1 6 [/SUP], Saima Yaqub[SUP] 1 [/SUP], Hassaan Bin Aslam[SUP] 1 [/SUP], Muhammad Waqar Aziz[SUP] 1 [/SUP], Tahir Yaqub[SUP] 7 [/SUP]
Affiliations
- PMID: 38687107
- DOI: 10.1637/aviandiseases-D-23-00029
in English, Spanish
The aim of the current study was to map the genetic diversity in the haemagglutinin (HA) glycoprotein of influenza A viruses (IAVs) of the H9N2 subtype. Twenty-five H9N2 IAVs were isolated from broiler chickens from March to July 2019. The HA gene was amplified, and phylogenetic analysis was performed to determine the evolutionary relationship. Important antigenic amino acid residues of HA attributed to immune escape and zoonotic potential were compared among H9N2 IAVs. Phylogenetic analysis revealed that sublineage B2 under the G1 lineage in Pakistan was found to be diversified, and newly sequenced H9N2 isolates were nested into two clades (A and B). Mutations linked to the antigenic variation and potential immune escape were observed as G72E (1/25, 4%), A180T (3/25, 12%), and A180V (1/25, 4%). A twofold significant reduction (P < 0.01) in log[SUB]2[/SUB] hemagglutination inhibition titers was observed with H9N2 IAV naturally harboring amino acid V180 instead of A180 in HA protein. Moreover, in the last 20 years, complete substitution at residues (T127D, D135N, and L150N) and partial substitution at residues (72, 74, 131, 148, 180, 183, 188, 216, 217, and 249, mature H9 HA numbering) associated with changes in antigenicity were observed. The presence of L216 in all H9N2 IAV isolates and T/V180 in four isolates in the receptor-binding site reveals the potential of these viruses to cross the species barrier to infect human or mammals. The current study observed the circulation of antigenically diverse H9N2 IAV variants that possess potential mutations that can escape the host immune system.
Keywords: H9N2 influenza A virus; HA protein; antigenic sites; mammalian adaptation; phylogenetic analysis; potential mutations.